2019年冠状病毒病(COVID-19)
大流行
抗原
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
2019-20冠状病毒爆发
糖蛋白
计算生物学
人口
蛋白质工程
生物
计算机科学
免疫学
医学
遗传学
生物化学
疾病
传染病(医学专业)
酶
病理
爆发
环境卫生
作者
Ching‐Lin Hsieh,Jason S. McLellan
标识
DOI:10.1016/j.sbi.2022.102385
摘要
Antigen design guided by high-resolution viral glycoprotein structures has successfully generated diverse vaccine candidates for COVID-19. Using conjugation systems to combine antigen design with computationally optimized nanoparticles, researchers have been able to display multivalent antigens with beneficial substitutions that elicited robust humoral immunity with enhanced neutralization potency and breadth. Here, we discuss strategies that have been used for structure-based design and nanoparticle display to develop COVID-19 vaccine candidates as well as potential next-generation vaccine candidates to protect against SARS-CoV-2 variants and other coronaviruses that emerge into the human population.
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